Linked Data
dbSNP Id:
rs1175339508
gnomAD v2:
1-229568430-C-T
gnomAD v3:
1-229432683-C-T
gnomAD v4:
1-229432683-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432683C>T , CM000663.2:g.229432683C>T | GRCh38 |
| NC_000001.10:g.229568430C>T , CM000663.1:g.229568430C>T | GRCh37 |
| NC_000001.9:g.227635053C>T | NCBI36 |
| NG_006672.1:g.6414G>A , LRG_429:g.6414G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.327G>A | ENSP00000355644.4:p.Glu109= | |
| ENST00000684723.1:c.192G>A | ENSP00000508084.1:p.Glu64= | |
| ENST00000366683.3:c.327G>A | ENSP00000355644.3:p.Glu109= | |
| ENST00000366684.7:c.327G>A MANE Select | ENSP00000355645.3:p.Glu109= | |
| NM_001100.3:c.327G>A , LRG_429t1:c.327G>A | NP_001091.1:p.Glu109= | |
| NM_001100.4:c.327G>A MANE Select | NP_001091.1:p.Glu109= |